Catalogue Number
BF-E4002
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
428.73
Appearance
White crystalline powder
Botanical Source
Aster tataricus
Structure Type
Terpenoids
Category
Standards;Natural Pytochemical;API
SMILES
CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O
Synonyms
epi-Friedelanol/Friedelan-3α-ol/(3R,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-octamethyldocosahydropicen-3-ol/(3R,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-Octamethyldocosahydro-3-picenol/(3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-Octamethyldocosahydropicen-3-ol/3Beta-Friedelanol/3-Picenol, docosahydro-4,4a,6b,8a,11,11,12b,14a-octamethyl-, (3R,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-/Epifriedelanol/3-Picenol, docosahydro-4,4a,6b,8a,11,11,12b,14a-octamethyl-, (3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-/3β-Friedelanol/3beta-Hydroxyfriedelane/(3S,4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS)-4,4a,6b,8a,11,11,12b,14a-Octamethyldocosahydro-3-picenol/Epifriendelanol/epifriedelenol
IUPAC Name
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol
Density
1.0±0.1 g/cm3
Solubility
Chloroform; Ethyl Acetate; Petroleum ether
Flash Point
199.6±12.3 °C
Boiling Point
478.3±13.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C30H52O/c1-20-21(31)9-10-22-27(20,5)12-11-23-28(22,6)16-18-30(8)24-19-25(2,3)13-14-26(24,4)15-17-29(23,30)7/h20-24,31H,9-19H2,1-8H3/t20-,21-,22+,23-,24+,26+,27+,28-,29+,30-/m0/s1
InChl Key
XCDQFROEGGNAER-PFOIMGGJSA-N
WGK Germany
RID/ADR
HS Code Reference
2906190000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:16844-71-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
MSDS
No Article Available.
Description :
Epifriedelanol is a triterpenoid isolated from the root bark of Ulmus davidiana, with antitumor activity[1]. Epifriedelanol inhibits cellular senescence in human primary cells[2].
